Microglia and Stem Cells for Ischemic Stroke Treatment-Mechanisms, Current Status, and Therapeutic Challenges

Aleksandra Markowska1, Dariusz Koziorowski1, Stanisław Szlufik1

  • 1Department of Neurology, Faculty of Health Sciences, Medical University of Warsaw, 03-242 Warsaw, Poland.

Insights

Neuroprotective therapies using microglia and stem cells show promise for ischemic stroke. Novel approaches like Muse cells and exosome therapy offer advantages over traditional treatments, addressing current limitations.

Area of Science:

  • Neuroscience
  • Regenerative Medicine
  • Biotechnology

Background:

  • Ischemic stroke is a leading cause of death and disability globally.
  • Current reperfusion therapies have significant limitations.
  • Research is exploring neuroprotective strategies involving microglia and stem cells.

Purpose of the Study:

  • To review the therapeutic effects of preconditioned microglia and stem cell-derived extracellular vesicles.
  • To elucidate the mechanisms of action, including bystander effect, exosome secretion, and biobridge formation.
  • To discuss preclinical and clinical findings, challenges, and potential solutions for stem cell therapies.

Main Methods:

  • Review of existing literature on microglia and stem cell therapies for ischemic stroke.
  • Analysis of mechanisms such as neurogenesis, angiogenesis, cell migration, and neuroinflammation modulation.
  • Examination of exosome-based therapy and novel stem cell types like Muse cells.

Main Results:

  • Stem cells (MSCs, NSCs, iPSCs, Muse cells) and microglia show neuroprotective potential.
  • Exosome therapy offers advantages over cell therapy, including lower immunogenicity and storage ease.
  • Preclinical studies show promise, but clinical translation faces challenges.

Conclusions:

  • Microglia and stem cell-derived factors, particularly exosomes, represent promising therapeutic avenues for ischemic stroke.
  • Muse cells offer a novel approach bypassing conventional stem cell limitations.
  • Further research and innovative strategies are needed to overcome clinical translation challenges in neuroprotection.